rs587781924
From SNPedia
Merged into | rs587778533 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587781924(-;T) |
Make rs587781924(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 2 |
Position | 47803559 |
Gene | MSH6 |
is a | snp |
is | mentioned by |
dbSNP | rs587781924 |
dbSNP (classic) | rs587781924 |
ClinGen | rs587781924 |
ebi | rs587781924 |
HLI | rs587781924 |
Exac | rs587781924 |
Gnomad | rs587781924 |
Varsome | rs587781924 |
LitVar | rs587781924 |
Map | rs587781924 |
PheGenI | rs587781924 |
Biobank | rs587781924 |
1000 genomes | rs587781924 |
hgdp | rs587781924 |
ensembl | rs587781924 |
geneview | rs587781924 |
scholar | rs587781924 |
rs587781924 | |
pharmgkb | rs587781924 |
gwascentral | rs587781924 |
openSNP | rs587781924 |
23andMe | rs587781924 |
SNPshot | rs587781924 |
SNPdbe | rs587781924 |
MSV3d | rs587781924 |
GWAS Ctlg | rs587781924 |
Status | Merged into rs587778533 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781924(T;T) |
Alt | rs587781924(T;T) |
Reference | Rs587781924(;) |
Significance | Pathogenic |
Disease | not specified Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MSH6 |
CLNDBN | not specified Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000002.11:g.48030698dupT |
CLNSRC | |
CLNACC | RCV000121582.1, RCV000130275.3, |